WO1993006793A1 - Implant femoral de hanche de rigidite reduite - Google Patents
Implant femoral de hanche de rigidite reduite Download PDFInfo
- Publication number
- WO1993006793A1 WO1993006793A1 PCT/US1992/008414 US9208414W WO9306793A1 WO 1993006793 A1 WO1993006793 A1 WO 1993006793A1 US 9208414 W US9208414 W US 9208414W WO 9306793 A1 WO9306793 A1 WO 9306793A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- stem
- groove
- proximal
- bone
- set forth
- Prior art date
Links
- 239000007943 implant Substances 0.000 title description 35
- 210000000988 bone and bone Anatomy 0.000 claims abstract description 51
- 229910001069 Ti alloy Inorganic materials 0.000 claims abstract description 10
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims abstract description 10
- WAIPAZQMEIHHTJ-UHFFFAOYSA-N [Cr].[Co] Chemical class [Cr].[Co] WAIPAZQMEIHHTJ-UHFFFAOYSA-N 0.000 claims abstract description 10
- 239000010936 titanium Substances 0.000 claims abstract description 10
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 10
- 238000002156 mixing Methods 0.000 claims abstract description 8
- 210000004394 hip joint Anatomy 0.000 claims abstract description 3
- 210000001624 hip Anatomy 0.000 claims description 14
- 210000000689 upper leg Anatomy 0.000 claims description 12
- 210000004197 pelvis Anatomy 0.000 claims description 4
- 210000003484 anatomy Anatomy 0.000 claims 1
- 229920000136 polysorbate Polymers 0.000 claims 1
- 238000004891 communication Methods 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 13
- 238000013461 design Methods 0.000 description 5
- 238000011882 arthroplasty Methods 0.000 description 3
- 238000011541 total hip replacement Methods 0.000 description 3
- 229930182556 Polyacetal Natural products 0.000 description 2
- 238000013459 approach Methods 0.000 description 2
- 238000003780 insertion Methods 0.000 description 2
- 230000037431 insertion Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229920006324 polyoxymethylene Polymers 0.000 description 2
- 238000007634 remodeling Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 229910000684 Cobalt-chrome Inorganic materials 0.000 description 1
- 208000032767 Device breakage Diseases 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- 230000008468 bone growth Effects 0.000 description 1
- 230000010072 bone remodeling Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000010952 cobalt-chrome Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 239000013013 elastic material Substances 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
Classifications
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- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L27/00—Materials for grafts or prostheses or for coating grafts or prostheses
- A61L27/50—Materials characterised by their function or physical properties, e.g. injectable or lubricating compositions, shape-memory materials, surface modified materials
- A61L27/56—Porous materials, e.g. foams or sponges
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2002/30014—Material related properties of the prosthesis or of a coating on the prosthesis the prosthesis being made from materials having different values of a given property at different locations within the same prosthesis differing in elasticity, stiffness or compressibility
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- A—HUMAN NECESSITIES
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- A61F2002/30316—The prosthesis having different structural features at different locations within the same prosthesis; Connections between prosthetic parts; Special structural features of bone or joint prostheses not otherwise provided for
- A61F2002/30317—The prosthesis having different structural features at different locations within the same prosthesis
- A61F2002/30322—The prosthesis having different structural features at different locations within the same prosthesis differing in surface structures
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
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- A61F2250/00—Special features of prostheses classified in groups A61F2/00 - A61F2/26 or A61F2/82 or A61F9/00 or A61F11/00 or subgroups thereof
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Definitions
- the present invention relates generally to a femoral hip prosthesis and, more particularly, to a femoral component having a stem which exhibits substantially controlled stiffness between its proximal and distal ends.
- the proximal femoral bone may ' resorb to a small fraction of its original mass, possibly causing a loss of support of the implant or implant breakage.
- implant flexural stiffness increases at an exponential rate, typically at powers between two and four, depending upon implant geometry, relative to linear increases in implant dimension.
- Further aggravating the situation is the fact that there is little correlation between the size of the patient and the diameter of the intramedullary canal. That is, a small, relatively light person may have a femur with a large diameter canal and a much larger person may have a femur with a smaller diameter canal. Therefore, it has been considered desirable to produce an implant, especially a larger diameter implant, with greatly reduced stiffness in relation to its stem diameter.
- the elasticity, and consequently the deformation, of an implant depends on the elastic modulus of the material and on the prosthetic design. By adjusting the physical characteristics of the foreign material to that of the bone tissue, as well as the design of the prosthesis to the femoral shaft, the entire system would have the same elasticity as a normal femur.
- a more elastic hip endoprosthesis also may act as a shock absorber during walking, particularly in the heel/strike and toe/off phases.”
- the prosthesis was composed of polyacetal resin which has an elasticity modulus approaching that of bone tissue, good durability, and tenacity for highly stressed components in combination with good tissue tolerance.
- the component was reinforced by a metallic core that was radiused toward the tip to increase the elasticity of the stem, thereby allowing the stem of the prosthesis to follow the deformation of the bone.
- Isoelasticity implies the optimum approximation of the physical characteristics of an implant to those of the bone.
- U.S. Patent No. 4,287,617 to Tornier discloses a hip prosthesis with a femoral stem which provides a measure of the elasticity spoken of by Morscher and Dick.
- a transverse section of the Tornier stem is in the form of a substantially rectangular tube of which one of the small sides is virtually cut away so as to leave a very large slot.
- the C-shaped section thus obtained is said to exhibit excellent transverse elasticity which facilitates the positioning of the pin in the medullary cavity by insertion.
- Other stated advantages are that the pin is not as heavy as solid designs, and that the cavity encourages bone growth.
- a femoral component of an artificial hip joint includes an elongated stem with a single longitudinally extending, generally medially facing, groove in its outer surface intermediate its proximal and distal ends.
- the dimensions of the groove are chosen so as to obtain a predetermined stiffness profile of the stem between the proximal and distal ends.
- the stem has a magnitude of stiffness no greater than that at which stress shielding of the first bone has been clinically identified by radiographic methods.
- the groove and the outer surface of the stem intersect at an outer rim.
- the groove has a central concave surface and proximal and distal radiused end surfaces in communication with and blending smoothly with the central cylindrical concave surface.
- the groove is disposed at an angle relative to the coronal plane, extending axially and can be angled either anteriorly or posteriorly to customize its stiffness.
- the component is preferably composed of cobalt-chromium alloy, but this principle is applicable to titanium or titanium alloy as well.
- the outer surface of the stem may be provided with a porous medium for encouraging bone ingrowth fixation.
- the invention enables the reduction of the stiffness of a femoral hip implant in a controlled fashion.
- the invention also maintains a controlled flexibility in the mid stem region while still affording extensive proximal and distal fixation.
- prior art components only allowed mid stem or distal flexibility while adversely reducing the potential fixation area.
- the neutral axis bending axis
- the femoral stem exhibiting the qualities of the invention may be composed of any of the common materials generally employed for implants. However, of these, titanium, titanium alloy, and cobalt chromium alloy would be preferable.
- FIG. 1 is a side elevation view, certain parts being cut away and shown in section, of a hip prosthesis, including a femoral component embodying the invention
- FIG. 2 is a perspective view of the femoral component of Fig. 1;
- FIG. 3 is a side elevation view of the femoral component, certain parts being cut away and shown in section;
- FIG. 4 is a top plan view of the femoral component
- FIG. 5 is a detail front elevation view of a portion of the femoral component
- FIG. 6 is a cross section view taken generally along line 6—6 in Fig. 5;
- FIG. 7 is a bar graph indicating relative stiffness of a series of stems of varying diameters for femoral components which are currently available commercially, as well as stems embodying the teachings of the present invention.
- FIG. 8 is a line graph generally depicting the information presented in Fig. 7. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
- FIG. l illustrates a hip prosthesis 20 including a femoral component 22 which embodies the invention.
- the femoral component 22 which may be of any material commonly used, such as a cobalt-chromium alloy, titanium, and titanium alloy, is suitably implanted in a femur 24 and is cooperatively engaged with an acetabular component 26. The latter component is suitably implanted in the acetabular cavity 28 of a pelvis 30.
- the femoral component 22 has a taper 32 at its extreme proximal end (Figs. 1-4) adapted to fittingly receive thereon a ball 34 (Fig. 1) .
- the ball is rotatably engaged with the acetabular component 26 in a known manner.
- the femoral component further includes a collar 36, with the taper 32 being joined to the shoulder via a neck 38.
- a stem 40 extends away from the collar 36 to a distal or tip end 42.
- the stem 40 is received in the intramedullary canal 44 (Fig. 1) of the femur and lies generally in the coronal plane of the body of the person in whom the prosthesis.is implanted.
- the lateral dimensions of the stem are substantially constant between the collar 36 at the proximal end and the distal end 42 of the femoral component 22.
- the stem is formed in any suitable manner with a single longitudinally extending groove 46 intermediate in its proximal and distal ends. As best seen in Figs. 3 and 5, the groove 46 includes a central concave surface 48 of substantially constant curvature as the stem is viewed in cross section (FIG. 6) and proximal and distal radiused end surfaces 50, 52, respectively.
- the central concave surface and the radiused end surfaces 50, 52 intersect with an outer surface 54 of the stem, the intersection occurring at an outer rim 56.
- the radiused end surfaces blend smoothly with the central concave surface 48 to prevent the occurrence of any undue stress concentrations.
- porous surface 58 enabling bone ingrowth fixation.
- An excellent example of such a surface results from application of the proprietary porous metal coating of DePuy Division of Boehringer Mannheim Corpora ⁇ tion provided under the trademark "POROCOAT".
- the porous surface 58 may be applied to specified portions of the outer surface 54.
- the shape and dimensions of the groove 46 are chosen so as to obtain substantially controlled stiffness of the stem 40 between its proximal and distal ends. Its purpose is to affect the mass moment of inertia of the femoral component at any given location along the length of the stem to thereby achieve a controlled stem flexibility.
- the shape of the cross section of the stem need not be circular but may include asymmetrical shapes, as desired, so long as substantially constant stem flexibility is maintained.
- the goal sought to be achieved by the stem 40 is that at all locations along its length it exhibits a magnitude of stiffness no greater than that at which stress shielding of the bone 24 would occur.
- the anatomic loading on the femoral component is determined, then the longitudinal axis of the groove is placed in the plane in which loading occurs.
- the groove 46 has a longitudinal axis parallel to the longitudinal axis of the stem and lies within a central bisecting plane which is generally angularly disposed relative to the coronal plane when the stem is implanted.
- the central bisecting plane of the longitudinally extending groove may be disposed at an angle within a range of 0° to approximately 45 relative to the coronal plane and extends axially, although a range of 0° to approximately 18° is preferred.
- the groove can be angled either anteriorly or posteriorly to customize its stiffness.
- FIG. 7 is a bar graph indicating relative stiffness of a series of stems of varying diameters ⁇ which are currently available for implanting. It is noteworthy that the 18 millimeter diameter stem exhibits approximately 10 times the stiffness of the 10.5 millimeter diameter stem.
- the invention serves to avoid this exponential increase. For example, as seen from the graph in FIG. 7, beginning with the 13.5 millimeter stem, if a 13.5mm diameter stem was determined as the adoptive remodling threshold, it would be desirable to maintain that stiffness on implants 13.5mm diameter and above.
- FIG. 8 is a line graph generally presenting the information of FIG. 7 in a different format.
- curve 60 represents the unmodified stem
- curve 62 represents the modified, constant moment, stem
- curve 64 represents the modified, variable moment, stem.
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Transplantation (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Dermatology (AREA)
- Cardiology (AREA)
- Engineering & Computer Science (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Vascular Medicine (AREA)
- Inorganic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Prostheses (AREA)
- Materials For Medical Uses (AREA)
Abstract
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU27871/92A AU680400B2 (en) | 1991-10-07 | 1992-10-02 | Reduced stiffness femoral hip implant |
DE69228190T DE69228190T2 (de) | 1991-10-07 | 1992-10-02 | Femorales hüftimplantat mit verringerter steifheit |
EP92921651A EP0607287B1 (fr) | 1991-10-07 | 1992-10-02 | Implant femoral de hanche de rigidite reduite |
CA002120706A CA2120706C (fr) | 1991-10-07 | 1992-10-02 | Implant de hanche a rigidite reduite |
JP50708893A JP3451257B2 (ja) | 1991-10-07 | 1992-10-02 | 低剛性大腿部股関節のインプラント |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US77302791A | 1991-10-07 | 1991-10-07 | |
US773,027 | 1991-10-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1993006793A1 true WO1993006793A1 (fr) | 1993-04-15 |
Family
ID=25096968
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US1992/008414 WO1993006793A1 (fr) | 1991-10-07 | 1992-10-02 | Implant femoral de hanche de rigidite reduite |
Country Status (7)
Country | Link |
---|---|
US (1) | US5336265A (fr) |
EP (1) | EP0607287B1 (fr) |
JP (1) | JP3451257B2 (fr) |
AU (1) | AU680400B2 (fr) |
CA (1) | CA2120706C (fr) |
DE (1) | DE69228190T2 (fr) |
WO (1) | WO1993006793A1 (fr) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1234556A2 (fr) * | 2001-02-23 | 2002-08-28 | Zimmer Inc. | Tige fémorale avec nervure de renforcement |
WO2003047471A1 (fr) * | 2001-11-30 | 2003-06-12 | Depuy International Limited | Piece femorale de prothese de hanche |
EP2886085A3 (fr) * | 2013-12-18 | 2015-10-07 | DePuy Synthes Products, LLC | Tige de prothèse orthopédique à module double |
US10213310B2 (en) | 2012-06-18 | 2019-02-26 | DePuy Synthes Products, Inc. | Dual modulus hip stem and method of making the same |
US10213314B2 (en) | 2013-03-14 | 2019-02-26 | DePuy Synthes Products, Inc. | Femoral component for an implantable hip prosthesis |
Families Citing this family (24)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0543099A3 (en) * | 1991-11-19 | 1994-05-25 | Bristol Myers Squibb Co | Implant fixation stem |
US5509935A (en) * | 1994-02-16 | 1996-04-23 | Wright Medical Technology, Inc. | Intramedullary implant with optimized geometric stiffness |
US5879398A (en) * | 1995-02-14 | 1999-03-09 | Zimmer, Inc. | Acetabular cup |
US5935172A (en) * | 1996-06-28 | 1999-08-10 | Johnson & Johnson Professional, Inc. | Prosthesis with variable fit and strain distribution |
US5755810A (en) * | 1996-11-13 | 1998-05-26 | Cunningham; Robert A. | Hip implant prosthesis |
US6913623B1 (en) | 2000-08-15 | 2005-07-05 | Centerpulse Orthopedics, Inc. | Two piecefused femoral hip stem |
US6682567B1 (en) | 2001-09-19 | 2004-01-27 | Biomet, Inc. | Method and apparatus for providing a shell component incorporating a porous ingrowth material and liner |
US6695883B2 (en) * | 2002-04-11 | 2004-02-24 | Theodore W. Crofford | Femoral neck fixation prosthesis |
US6755866B2 (en) | 2002-08-20 | 2004-06-29 | Depuy Products, Inc. | Prosthetic stem with bearings |
US6887278B2 (en) * | 2002-11-04 | 2005-05-03 | Mayo Foundation For Medical Education And Research | Prosthetic implant having segmented flexible stem |
US7534271B2 (en) | 2004-01-22 | 2009-05-19 | Smith + Nephew | Femoral hip prosthesis and method of implantation |
US7547328B2 (en) * | 2004-05-26 | 2009-06-16 | Sidebotham Christopher G | Canine femoral stem system |
US7892290B2 (en) * | 2004-05-28 | 2011-02-22 | Smith & Nephew, Inc. | Fluted sleeve hip prosthesis for modular stem |
WO2005117763A2 (fr) * | 2004-05-28 | 2005-12-15 | Smith & Nephew, Inc. | Tige intramedullaire cannelee |
EP2068772A2 (fr) * | 2006-09-20 | 2009-06-17 | Smith & Nephew, Inc. | Tige à rigidité variable pour implants prothétiques |
US20080287958A1 (en) * | 2007-05-14 | 2008-11-20 | Howmedica Osteonics Corp. | Flexible intramedullary rod |
US9949837B2 (en) | 2013-03-07 | 2018-04-24 | Howmedica Osteonics Corp. | Partially porous bone implant keel |
KR102168619B1 (ko) * | 2017-08-07 | 2020-10-22 | 옌 왕 | 선천성고관절발육불량 치료용 코브라 형상 대퇴스템삽입물 |
KR102168618B1 (ko) * | 2017-08-07 | 2020-10-22 | 옌 왕 | 인공α대퇴스템삽입물 |
US10206782B1 (en) | 2017-10-12 | 2019-02-19 | King Saud University | Custom-fitting collar sleeve backing for commercial hip protheses |
US11123085B2 (en) | 2018-04-11 | 2021-09-21 | Howmedica Osteonics Corp. | Cutting tool positioned by flexible rod for revision surgery |
JP2021115433A (ja) * | 2020-01-23 | 2021-08-10 | 株式会社シミズテック | 人工股関節用ステム |
CN113081402B (zh) * | 2021-03-31 | 2021-11-05 | 北京航空航天大学 | 一种股骨柄假体 |
CN117257529B (zh) * | 2023-11-21 | 2024-02-09 | 北京力达康科技有限公司 | 一种钽涂层髋关节假体系统 |
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- 1992-10-02 JP JP50708893A patent/JP3451257B2/ja not_active Expired - Lifetime
- 1992-10-02 CA CA002120706A patent/CA2120706C/fr not_active Expired - Lifetime
- 1992-10-02 EP EP92921651A patent/EP0607287B1/fr not_active Expired - Lifetime
- 1992-10-02 AU AU27871/92A patent/AU680400B2/en not_active Expired - Fee Related
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Cited By (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1234556A2 (fr) * | 2001-02-23 | 2002-08-28 | Zimmer Inc. | Tige fémorale avec nervure de renforcement |
EP1234556A3 (fr) * | 2001-02-23 | 2004-03-03 | Zimmer Inc. | Tige fémorale avec nervure de renforcement |
EP1652496A3 (fr) * | 2001-02-23 | 2007-04-25 | Zimmer Inc. | Tige fémorale avec nervure de renforcement |
WO2003047471A1 (fr) * | 2001-11-30 | 2003-06-12 | Depuy International Limited | Piece femorale de prothese de hanche |
US10213310B2 (en) | 2012-06-18 | 2019-02-26 | DePuy Synthes Products, Inc. | Dual modulus hip stem and method of making the same |
US11020232B2 (en) | 2012-06-18 | 2021-06-01 | DePuy Synthes Products, Inc. | Dual modulus hip stem and method of making the same |
US10213314B2 (en) | 2013-03-14 | 2019-02-26 | DePuy Synthes Products, Inc. | Femoral component for an implantable hip prosthesis |
US11058543B2 (en) | 2013-03-14 | 2021-07-13 | DePuy Synthes Products, Inc. | Femoral component for an implantable hip prosthesis and method of making same |
EP2886085A3 (fr) * | 2013-12-18 | 2015-10-07 | DePuy Synthes Products, LLC | Tige de prothèse orthopédique à module double |
Also Published As
Publication number | Publication date |
---|---|
EP0607287B1 (fr) | 1999-01-13 |
EP0607287A4 (fr) | 1995-02-22 |
US5336265A (en) | 1994-08-09 |
DE69228190T2 (de) | 1999-09-23 |
JPH08503859A (ja) | 1996-04-30 |
CA2120706A1 (fr) | 1993-04-15 |
AU2787192A (en) | 1993-05-03 |
AU680400B2 (en) | 1997-07-31 |
CA2120706C (fr) | 2003-06-17 |
EP0607287A1 (fr) | 1994-07-27 |
DE69228190D1 (de) | 1999-02-25 |
JP3451257B2 (ja) | 2003-09-29 |
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